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Connect your variants of interest with real-world clinician activity, turning search data into actionable insight for faster recruitment, smarter site selection, and targeted outreach. See who is working with your variants, where and how, so you can focus resources where they matter most.
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What Insights?
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Clinician Engagement

Learn which clinicians are searching your variants, how they classify them, and which organisations they represent. Understand who is most active in your disease area.
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Geographic Prevalence

See where interest in your variants is highest across the globe. Use search activity to identify regions with likely disease prevalence and better plan outreach or trials.
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Emerging Trends

Track historical and real-time search data for your variants. Spot rising interest and detect newly recognised cases early, helping you adjust recruitment and strategy.
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Targeted Outreach

Connect with clinicians who have searched for your variants and consented to be contacted. Deliver the right information at the right time to accelerate engagement, and place native ads directly on VarSome gene and variant pages to reach clinicians in the context of their search.
Why VarSome?

VarSome.com attracts over 500,000 page views per month from healthcare professionals across six continents. With Insights, you can place your message directly in front of the clinicians and researchers already engaging with your variants of interest, ensuring visibility where it matters most.

Use real-world search activity to track disease prevalence and identify where patients are most likely to be found. VarSome Insights helps you pinpoint candidate sites and connect with clinicians working in those regions, streamlining recruitment and supporting smarter trial planning.

Join one of the world’s largest networks of clinical geneticists and healthcare professionals. VarSome Insights lets you tap into live data from this global community, helping you collaborate, share knowledge, and strengthen clinical programmes with insights gathered across more than 150 countries.

Over 87% of VarSome users have consented to be contacted for relevant trials and therapies. With VarSome Insights, you can reach out directly to clinicians who have shown interest in your variants, opening a dialogue that leads to faster engagement and stronger partnerships.

Insights go beyond reporting. Whether it’s contacting clinicians who have searched for your variants or placing targeted messages on VarSome result pages, you can translate data into meaningful engagement that accelerates clinical development.

VarSome Insights provides both retrospective and real-time reporting on your variants of interest. Retrospective reports look back up to two years, revealing historical search patterns and past clinical interest. Active weekly reports keep you up to date with current activity, highlighting where new searches are happening and where patients may be emerging. Together, these reports give you the historical context and real-time perspective needed to support recruitment, site selection, and clinician outreach.

Prevalence Inferrance Use Case

ASAH1 Prevalence from Real-World Search Data

Using VarSome Insights, researchers at Aceragen and Saphetor analyzed two years of ASAH1 gene queries to infer that ASAH1-related diseases are more prevalent than previously reported. The poster shows how search volume can reveal case activity in underrepresented regions and supports early decision-making in rare disease research. Dive into this work to see how VarSome Insights turns search metadata into meaningful epidemiology.

See The Poster
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What Do Our Partners Say?

Successful Clinical Trial Enrolment
"We had another person agree to participate in our clinical trial.
That's a great record of success."

Disease Prevalence Mapping
"Traditional prevalence efforts are usually a costly and timely endeavor.
Inferred prevalence may circumvent this spend during early
development efforts."

Rare Disease Awareness
"We look forward to leveraging Saphetor's innovative approach
to bring together the global genomics community to build awareness
in our rare disease program."

Find Out How We Can Help